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Volume 35; Issue 1
Main
Ophthalmic Genetics
Volume 35; Issue 1
Ophthalmic Genetics
Volume 35; Issue 1
1
Complement Factor B Polymorphism and the Phenotype of Early Age-related Macular Degeneration
Mantel, Irmela
,
Ambresin, Aude
,
Moetteli, Leila
,
Droz, Ivaine
,
Roduit, Raphaël
,
Munier, Francis L.
,
Schorderet, Daniel F.
Journal:
Ophthalmic Genetics
Year:
2014
Language:
english
File:
PDF, 131 KB
Your tags:
english, 2014
2
The Prevalence of Macular Cysts in Patients with Clinical Cone-Rod Dystrophy Determined by Spectral-Domain Optical Coherence Tomography
Salvatore, Serena
,
Genead, Mohamed A.
,
Fishman, Gerald A.
Journal:
Ophthalmic Genetics
Year:
2014
Language:
english
File:
PDF, 411 KB
Your tags:
english, 2014
3
VKORC1 C1173T and VKORC1 G-1639A Gene Polymorphisms in Turkish Behçet’s Patients with Ocular and Non-ocular Involvement
Demir, Helin Deniz
,
Ortak, Hüseyin
,
Şahin, Şemsettin
,
Ateş, Ömer
,
Benli, İsmail
,
İnanır, Ahmet
Journal:
Ophthalmic Genetics
Year:
2014
Language:
english
File:
PDF, 127 KB
Your tags:
english, 2014
4
The Protective Role of the −735C/T and the −1306C/T Polymorphisms of the MMP-2 Gene in the Development of Primary Open-angle Glaucoma
Kaminska, Anna
,
Banas-Lezanska, Patrycja
,
Przybylowska, Karolina
,
Gacek, Mira
,
Majsterek, Ireneusz
,
Szaflik, Jerzy
,
Szaflik, Jacek P.
Journal:
Ophthalmic Genetics
Year:
2014
Language:
english
File:
PDF, 134 KB
Your tags:
english, 2014
5
Report of a Novel Mutation in CRB1 in a Lebanese Family Presenting Retinal Dystrophy
Jalkh, Nadine
,
Guissart, Claire
,
Chouery, Eliane
,
Yammine, Tony
,
Ali, Nagham El
,
Farah, Hanane Abi
,
Mégarbané, André
Journal:
Ophthalmic Genetics
Year:
2014
Language:
english
File:
PDF, 789 KB
Your tags:
english, 2014
6
Xq26.3 Microdeletion in a Male with Wildervanck Syndrome
Abu-Amero, Khaled K.
,
Kondkar, Altaf A.
,
Alorainy, Ibrahim A.
,
Khan, Arif O.
,
Al-Enazy, Leila A.
,
Oystreck, Darren T.
,
Bosley, Thomas M.
Journal:
Ophthalmic Genetics
Year:
2014
Language:
english
File:
PDF, 797 KB
Your tags:
english, 2014
7
Sequencing Analysis of the ATOH7 Gene in Individuals with Optic Nerve Hypoplasia
Lim, Sing-Hui
,
Germain, Elizabeth St.
,
Tran-Viet, Khanh-Nhat
,
Staffieri, Sandra
,
Marino, Meghan
,
Dollfus, Pr Hélène
,
Nading, Erica B.
,
Crowe, Sue
,
Gole, Glen
,
Perdomo-Trujillo, Yaumara
,
Haybittel, Mic
Journal:
Ophthalmic Genetics
Year:
2014
Language:
english
File:
PDF, 118 KB
Your tags:
english, 2014
8
Sorting out Co-occurrence of Rare Monogenic Retinopathies: Stargardt Disease Co-existing with Congenital Stationary Night Blindness
Huynh, Nancy
,
Jeffrey, Brett G.
,
Turriff, Amy
,
Sieving, Paul A.
,
Cukras, Catherine A.
Journal:
Ophthalmic Genetics
Year:
2014
Language:
english
File:
PDF, 859 KB
Your tags:
english, 2014
9
Clinical Phenotype in Ten Unrelated Japanese Patients with Mutations in the EYS Gene
Suto, Kimiko
,
Hosono, Katsuhiro
,
Takahashi, Masayo
,
Hirami, Yasuhiko
,
Arai, Yuki
,
Nagase, Yasunori
,
Ueno, Shinji
,
Terasaki, Hiroko
,
Minoshima, Shinsei
,
Kondo, Mineo
,
Hotta, Yoshihiro
Journal:
Ophthalmic Genetics
Year:
2014
Language:
english
File:
PDF, 641 KB
Your tags:
english, 2014
10
TBK1 and Flanking Genes in Human Retina
Fingert, John H.
,
Darbro, Benjamin W.
,
Qian, Qining
,
Van Rheeden, Richard
,
Miller, Kathy
,
Riker, Megan
,
Solivan-Timpe, Frances
,
Roos, Ben R.
,
Robin, Alan L.
,
Mullins, Robert F.
Journal:
Ophthalmic Genetics
Year:
2014
Language:
english
File:
PDF, 512 KB
Your tags:
english, 2014
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